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作 者:赵元晖[1] 李八方[1] 马敬军 董士远[1] 刘尊英[1] 曾名湧[1]
机构地区:[1]中国海洋大学食品科学与工程学院,青岛266003 [2]中国检验认证集团山东有限公司,青岛266071
出 处:《高等学校化学学报》2012年第2期308-312,共5页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:31000830);山东省自然科学基金(批准号:ZR2010CQ001)资助
摘 要:采用Sephadex G-25凝胶柱层析、SP Sephadex C-25阳离子交换层析和反相高效液相色谱等方法对海地瓜水解产物进行分离纯化,得到了一种新的强活性ACE抑制肽,其氨基酸序列为MEGAQEAQGD,IC50值为15.9μmol/L.采用逐步缩合和片段缩合的方法对该抑制肽进行了设计合成.合成肽的纯度为99.72%,分子量与序列结构均与理论值相符.研究发现,抑制肽与胃蛋白酶和糜蛋白酶水解反应后,活性增强了3.5倍.动物实验结果表明,剂量为3μmol/kg的抑制肽对大鼠自发性高血压具有明显的降压效果.A novel ACE inhibitory peptide was isolated from the sea cucumber(Acaudina molpadioidea) hydrolysate using the chromatographic methods including gel filtration,ion-exchange chromatography and reversed phase high-performance liquid chromatography.The purified ACE inhibitory peptide was sequenced as MEGAQEAQGD,with a IC50 value of 15.9 μmol/L.The ACE inhibitory peptide was synthesized by a method of gradual condensation and fragmental condensation.The purity of the decapeptide was 99.72%,and the molecular weight and sequence structure of the decapeptide equate with the fact.It was found that the inhibitory activity of the peptide was intensified by 3.5 times after incubation with pepsin and chymotrypsin.The ACE inhibitory peptide from Acaudina molpadioidea showed a clear antihypertensive effect on spontaneously hypertensive rats(SHR),at a dosage of 3 μmol/kg.
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